US1648941A - Manufacture of oxide-coated cathodes - Google Patents
Manufacture of oxide-coated cathodes Download PDFInfo
- Publication number
- US1648941A US1648941A US123031A US12303126A US1648941A US 1648941 A US1648941 A US 1648941A US 123031 A US123031 A US 123031A US 12303126 A US12303126 A US 12303126A US 1648941 A US1648941 A US 1648941A
- Authority
- US
- United States
- Prior art keywords
- coating
- oxide
- carbonates
- manufacture
- filament
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000004519 manufacturing process Methods 0.000 title description 8
- 238000000576 coating method Methods 0.000 description 21
- 239000011248 coating agent Substances 0.000 description 20
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 11
- 239000012286 potassium permanganate Substances 0.000 description 9
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 8
- 150000001342 alkaline earth metals Chemical class 0.000 description 7
- 239000000725 suspension Substances 0.000 description 7
- 239000000463 material Substances 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- 239000007900 aqueous suspension Substances 0.000 description 3
- 239000008199 coating composition Substances 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 238000005247 gettering Methods 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 238000005299 abrasion Methods 0.000 description 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 2
- 230000027455 binding Effects 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 230000002939 deleterious effect Effects 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- IATRAKWUXMZMIY-UHFFFAOYSA-N strontium oxide Chemical compound [O-2].[Sr+2] IATRAKWUXMZMIY-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Inorganic materials [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 1
- AYJRCSIUFZENHW-DEQYMQKBSA-L barium(2+);oxomethanediolate Chemical compound [Ba+2].[O-][14C]([O-])=O AYJRCSIUFZENHW-DEQYMQKBSA-L 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000005587 carbonate group Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- BDAGIHXWWSANSR-NJFSPNSNSA-N hydroxyformaldehyde Chemical compound O[14CH]=O BDAGIHXWWSANSR-NJFSPNSNSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- HWLDNSXPUQTBOD-UHFFFAOYSA-N platinum-iridium alloy Chemical compound [Ir].[Pt] HWLDNSXPUQTBOD-UHFFFAOYSA-N 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 229910000018 strontium carbonate Inorganic materials 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J9/00—Apparatus or processes specially adapted for the manufacture, installation, removal, maintenance of electric discharge tubes, discharge lamps, or parts thereof; Recovery of material from discharge tubes or lamps
- H01J9/02—Manufacture of electrodes or electrode systems
- H01J9/04—Manufacture of electrodes or electrode systems of thermionic cathodes
- H01J9/042—Manufacture, activation of the emissive part
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/294—Coated or with bond, impregnation or core including metal or compound thereof [excluding glass, ceramic and asbestos]
- Y10T428/2958—Metal or metal compound in coating
Definitions
- This invention relates to cathodes for electron discharge devices employing as the active electron emissive material a coating of the oxides of the alkaline earth metals as, for instance, a mixture of barium and strontium oxide.
- the cathode After the cathode is enclosed in the evacuated envelope it is heated by passage of current therethrough to convert the carbonates to the oxide and thereby render the cathode thermionically active. It has been found that decidedly superior life and emission are obtained when the carbonate coating of the filament is not decomposed prior to its inclusion in the evacuated envelope. The carbonates moreover are extremely stable in air and the filaments coated therewith may be stocked for long periods of time without deleterious contamination or alteration of the emissive properties thereof.
- a coating of the carbonates of the alkaline earth metals is obtained by applying the same from an aqueous suspension of the alkaline earth carbonates, each coating so applied being baked onto the filament. Any desired number of coatings may beapplied depending upon the consistency of the suspension and the Weight of coating required on the filament.
- the present invention is concerned with the production of a cathode in accordance with the process of the MacRae application, an object of the invention being to cause a. firm adherence of the carbonates to the me- Application filed July is, 1926. Serial No. 123,031.
- a coating composition which we have found to be particularly efficacious in the production of oxide coated cathodes is as follows:
- the materials are thoroughly mixed and applied to the filament in any suitable manner, such as by spraying,'dipping, or painting but preferably the filament is drawn through the suspension in a continuous manner.
- a gettering cup such as ordinarily employed in the incandescent lamp industry, the filament being passed through the gettering cup in the usual manner and through a baking oven preferably in the form of a tube furnace in which the coating is baked onto the metallic core.
- An atmosphere of carbon dioxide is provided for the furnace to prevent decomposition of the carbonate coating and the temperature of the furnace is adjusted to about 1000 C.
- the potassium 'perinan anate serves in some manner not fully understood to bind the coating to the wire and prevent the same from flaking or-rubbing off during the subsequent handling.
- the binding action may be due to the tendency of the soluble salt, that is. the potassium permanganate, to crystallize out of the suspension in which it is in solution and due to the formation of such crystais'to assist in bonding the coating to the Wire.
- the crystal so formed would also strengthen and toughen the coating.
- Potassium permanganate has a needle-like employing potassium permanganate crystal structure of such form that the ad- .jac'ent crystals tend to' interlock with each other and thereb form a mass which is strong and capab e of holdingithe carbonates firmly to the metal core and While the potassium perman anate is decomposed by the baking heat it is thought that the beneficial influence of the crystal form may be retained in thecompletedcoating.
- potassium permanganate has been specified as the preferred material it is to be understood that other soluble; salts which crystallize out of solution or which have a fusion temperature below the baking temperature of the coating and which exert no deleterious influence on the emission of the cathode may be employed and we do not desire to be limited to the specific material suggested, nor to the exact proportions specified since many changes may be made there in without departing from the invention.
- a coating composition fOllZllB production of thermionically active bodies comprising a suspension of alkaline earth carbonates having in solution potassium permanganate.
- a coating composition for the production of thermionically active bodies comprising amixture of the carbonates of barium and strontium in an aqueous suspension con taining a small percentage of potassium permanganate.
- thermoionically active bodies which comprises coating ametallic base member with a suspension of a compound of an alkaline earth metal containing a soluble salt and baking the coating onto the filament ata temperature sufficient to crystallize out said salt and fuse the same.
- the method of producing thermionically active bodies which comprises coating a metallic base member with a suspension of a compound of an alkaline earth metal containing potassium. permanganate.
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Solid Thermionic Cathode (AREA)
Description
Patented Nov. 15, 1927.
sures 1,648,941 PATENT OFFICE.
WILLIAM BENJAMIN GERO AND GEORGE WILSON HALLOCK, OF BLOOMFIELD, NEW JERSEY, ASSIGNORS, TO WESTINGHOUSE LAMP COMPANY, A CORPORATION OF PENNSYLVANIA.
MANUFACTURE OE OXIDE-COATED CATHODES;
No Drawing.
This invention relates to cathodes for electron discharge devices employing as the active electron emissive material a coating of the oxides of the alkaline earth metals as, for instance, a mixture of barium and strontium oxide.
In the manufacture of cathodes of the above nature it is the customary practice to coat a metallic base such as a platinum iridium filament with a compound of the alkaline earth metals other than the oxide and to convert the same to the oxide either before or after sealing ofthe cathode into an envelope of the device.
In an application of Duncan MacR-ae, Se-
rial No. 587,270, filed September 11, 1922, entitled Electron-emitting devices and method of making and assigned to the VVestinghouse Lamp Company there is disclosed a' method of coating a metallic base material with the carbonates of the alkaline earth metals, such compound being baked onto the filament in the presence of carbon dioxide in order to prevent decomposition thereof or conversion of the carbonates to the oxide.
After the cathode is enclosed in the evacuated envelope it is heated by passage of current therethrough to convert the carbonates to the oxide and thereby render the cathode thermionically active. It has been found that decidedly superior life and emission are obtained when the carbonate coating of the filament is not decomposed prior to its inclusion in the evacuated envelope. The carbonates moreover are extremely stable in air and the filaments coated therewith may be stocked for long periods of time without deleterious contamination or alteration of the emissive properties thereof.
According to the process set forth in the application of MacRae supra, a coating of the carbonates of the alkaline earth metals is obtained by applying the same from an aqueous suspension of the alkaline earth carbonates, each coating so applied being baked onto the filament. Any desired number of coatings may beapplied depending upon the consistency of the suspension and the Weight of coating required on the filament.
The present invention is concerned with the production of a cathode in accordance with the process of the MacRae application, an object of the invention being to cause a. firm adherence of the carbonates to the me- Application filed July is, 1926. Serial No. 123,031.
tallic core so that they will resist abrasion and handling during factory manipulations such as mounting.
Other objects and advantages will hereinafter appear.
We have found that when a soluble salt such as potassium permanganate is added to the aqueous suspension in the proper proportion that it greatly facilitates the coating operation making the resulting coating adhere very much better to the metallic base. A coating composition which we have found to be particularly efficacious in the production of oxide coated cathodes is as follows:
Barium carbonate, 8- grams; strontium carbonate, 8 grams; potassium permanganate, 30 cc. of a 2% aqueous solution.
The materials are thoroughly mixed and applied to the filament in any suitable manner, such as by spraying,'dipping, or painting but preferably the filament is drawn through the suspension in a continuous manner. This may be conveniently carried out by the use of a gettering cup such as ordinarily employed in the incandescent lamp industry, the filament being passed through the gettering cup in the usual manner and through a baking oven preferably in the form of a tube furnace in which the coating is baked onto the metallic core. An atmosphere of carbon dioxide is provided for the furnace to prevent decomposition of the carbonate coating and the temperature of the furnace is adjusted to about 1000 C.
Due to the tendency of the carbonates to settle out of the suspension, it is necessary to agitate the solution continuously, such agitation being accomplished with the apparatus set forth above by the rotation of the gettering wheel.
During the/baking of the coating the potassium 'perinan anate serves in some manner not fully understood to bind the coating to the wire and prevent the same from flaking or-rubbing off during the subsequent handling. The binding action may be due to the tendency of the soluble salt, that is. the potassium permanganate, to crystallize out of the suspension in which it is in solution and due to the formation of such crystais'to assist in bonding the coating to the Wire. The crystal so formed would also strengthen and toughen the coating. Potassium permanganate has a needle-like employing potassium permanganate crystal structure of such form that the ad- .jac'ent crystals tend to' interlock with each other and thereb form a mass which is strong and capab e of holdingithe carbonates firmly to the metal core and While the potassium perman anate is decomposed by the baking heat it is thought that the beneficial influence of the crystal form may be retained in thecompletedcoating.
Another possible explanation of the binding action is the fusion of the soluble salt or. of its products of decomposition when heat is applied thereto, resultlng in the roduotion of afused mass in which the car onates are held by a mechanical bond in such manner that they resist abrasion. \Vhatever the true explanation, the fact remains that when or equivalentsalts a much better bonding of the coating material onto the wire results.
While potassium permanganate has been specified as the preferred material it is to be understood that other soluble; salts which crystallize out of solution or which have a fusion temperature below the baking temperature of the coating and which exert no deleterious influence on the emission of the cathode may be employed and we do not desire to be limited to the specific material suggested, nor to the exact proportions specified since many changes may be made there in without departing from the invention.
What is claimed is:
1'.'A coating composition-for the production of thermionically active bodies comprising a compound of alkaline earth metal or metals in a suspending medium containing potassium permanganate.
2. A coating composition fOllZllB production of thermionically active bodies comprising a suspension of alkaline earth carbonates having in solution potassium permanganate.
3. A coating composition for the production of thermionically active bodies comprising amixture of the carbonates of barium and strontium in an aqueous suspension con taining a small percentage of potassium permanganate.
4. The method of producing thermionically active bodies which comprises coating ametallic base member with a suspension of a compound of an alkaline earth metal containing a soluble salt and baking the coating onto the filament ata temperature sufficient to crystallize out said salt and fuse the same. y Y
5. The method of producing thermionically active bodies which comprises coating a metallic base member with a suspension of a compound of an alkaline earth metal containing potassium. permanganate.
In testimony whereof, We have hereunto subscribed our names this 14th day of July,
WILLIAM BENJAMIN GERO. GEORGE WILSON HALLOOK.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US123031A US1648941A (en) | 1926-07-16 | 1926-07-16 | Manufacture of oxide-coated cathodes |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US123031A US1648941A (en) | 1926-07-16 | 1926-07-16 | Manufacture of oxide-coated cathodes |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1648941A true US1648941A (en) | 1927-11-15 |
Family
ID=22406335
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US123031A Expired - Lifetime US1648941A (en) | 1926-07-16 | 1926-07-16 | Manufacture of oxide-coated cathodes |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1648941A (en) |
-
1926
- 1926-07-16 US US123031A patent/US1648941A/en not_active Expired - Lifetime
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